chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109064690090646901AG7GENIChomozygous116676811
109064938990649390TC11GENIChomozygous116676813
109065069790650698TA5GENIChomozygous116676815
109065209590652096TC5GENIChomozygous116676817
109065317990653180GA10GENIChomozygous116676819
109065530490655305CT16GENIChomozygous116676821
109065561490655615CG18GENIChomozygous116676823
109065608190656082AT12GENIChomozygous116676825
109065636990656370GT13GENIChomozygous116676827
109065707190657072AG6GENIChomozygous116676829
109065707290657073CT6GENIChomozygous116676831
109065765690657657AG14GENIChomozygous116676833
109065785090657851GT9GENIChomozygous116676835
109065800490658005AG8GENIChomozygous116676837
109065789290657893CT10GENIChomozygous116821029
109065788890657889GA10GENIChomozygous116821027